pulmonary fibrosis
Chronic progressive interstitial lung disorder characterized by the replacement of the lung tissue by connective tissue, leading to progressive dyspnea, respiratory failure, or right heart failure. Causes include chronic inflammatory processes, exposure to environmental irritants, radiation therapy, autoimmune disorders, certain drugs, or it may be idiopathic (no identifiable cause). [ NCIT:P378 ]
Term info
- DOID:3770 (MONDO:equivalentTo)
- NCIT:C26869 (MONDO:equivalentTo)
- MESH:D011658 (MONDO:equivalentTo)
- SCTID:51615001 (MONDO:equivalentTo)
- UMLS:C0034069 (NCIT:C26869)
Chronic progressive interstitial lung disorder characterized by the replacement of the lung tissue by connective tissue, leading to progressive dyspnea, respiratory failure, or right heart failure. Causes include chronic inflammatory processes, exposure to environmental irritants, radiation therapy, autoimmune disorders, certain drugs, or it may be idiopathic (no identifiable cause).
http://identifiers.org/snomedct/51615001, http://purl.obolibrary.org/obo/NCIT_C26869, http://purl.obolibrary.org/obo/DOID_3770, http://linkedlifedata.com/resource/umls/id/C0034069, http://identifiers.org/mesh/D011658
fibrosis of lung, pulmonary interstitial fibrosis
MONDO:0002771